What are the responsibilities and job description for the Clinical Research Coordinator (part-time) position at Joulé?
Job Title: Clinical Research Coordinator (Part-Time)
Location: New Haven, CT
Type: Contract
Compensation: $36 - $45 hourly
Contractor Work Model: Onsite
Position Overview
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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Ref: #568-Clinical
Location: New Haven, CT
Type: Contract
Compensation: $36 - $45 hourly
Contractor Work Model: Onsite
Position Overview
We are seeking a detail-oriented and experienced Clinical Research Coordinator (CRC) to support a data clean-up initiative for an ongoing study. This is a part-time role focused heavily on Electronic Data Capture (EDC) and ensuring the accuracy and completeness of patient data. The ideal candidate will have a strong background in clinical research and data management, with a passion for quality and compliance.
Key Responsibilities- Perform comprehensive data review and clean-up in EDC systems for ongoing clinical trials.
- Ensure all patient data is accurate, complete, and compliant with study protocols and GCP guidelines.
- Collaborate with study teams to resolve data queries and discrepancies.
- Support monitoring visits and assist with query resolution.
- Maintain accurate visit logs and update CTMS visit statuses.
- Communicate effectively with site staff and sponsor representatives.
- Provide high-quality support to ensure smooth study operations.
- Bachelor’s degree in a health-related or scientific field required.
- Must have oncology experience.
- 3–5 years of experience in a clinical research setting, preferably as a CRC.
- Strong proficiency in EDC platforms and clinical data management.
- Excellent organizational skills and attention to detail.
- Strong verbal and written communication skills.
- Ability to work independently and manage time effectively.
System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M-
#DI-
Ref: #568-Clinical
Salary : $36 - $45